van Leyen Klaus, Arai Ken, Jin Guang, Kenyon Victor, Gerstner Bettina, Rosenberg Paul A, Holman Theodore R, Lo Eng H
Neuroprotection Research Laboratory, Massachusetts General Hospital, Charlestown, Massachusetts 02129, USA.
J Neurosci Res. 2008 Mar;86(4):904-9. doi: 10.1002/jnr.21543.
The lipid-metabolizing enzyme 12/15-lipoxygenase (12/15-LOX) mediates cell death resulting from oxidative stress in both neurons and oligodendrocytes. Specifically, it may contribute to the pathophysiology of stroke and Alzheimer's and Parkinson's diseases. We report here that two of three specific 12/15-LOX inhibitors, derived from a virtual screen by computer modeling and validated by inhibition of recombinant human 15-LOX in vitro, are able to rescue both neuronal as well as oligodendroglial cells from cell death induced by oxidative stress. Thus, in a fairly streamlined process, an initial virtual screen of 50,000 compounds in a library of drug-like molecules has led to the identification of two novel drug candidates for targeting LOX. Future studies of these novel neuroprotective inhibitors of 12/15-LOX may provide new therapeutic opportunities to combat stroke and other neurodegenerative diseases.
脂质代谢酶12/15-脂氧合酶(12/15-LOX)介导神经元和少突胶质细胞中氧化应激导致的细胞死亡。具体而言,它可能与中风、阿尔茨海默病和帕金森病的病理生理学有关。我们在此报告,通过计算机建模进行虚拟筛选并经体外抑制重组人15-LOX验证得到的三种特异性12/15-LOX抑制剂中的两种,能够使神经元和少突胶质细胞从氧化应激诱导的细胞死亡中获救。因此,在一个相当简化的过程中,对一个类药物分子库中的50000种化合物进行初步虚拟筛选,已鉴定出两种靶向LOX的新型候选药物。对这些新型12/15-LOX神经保护抑制剂的进一步研究可能会为对抗中风和其他神经退行性疾病提供新的治疗机会。